21 CFR 556.226
§ 556.226 Enrofloxacin.
United States · 21 CFR — Food and Drugs · Status: effective
Cite this
- Citation
- 21 CFR 556.226, § 556.226 Enrofloxacin, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/87761
- Permanent ID
ys:prov:87761@1- SHA-256
69ee979300067cd1b2173ecd893181ed91e7f9ce7e9d6879dafa3278ead628bb
The hash is SHA-256 of this version's text, with every run of whitespace collapsed to a single space and the ends trimmed. The ID always leads back here, and checking it says whether the text you cited is still the current version.
Full text
(a) Acceptable daily intake (ADI). The ADI for total residue of enrofloxacin is 3 µg/kg of body weight per day.
(b) Tolerances. The tolerances for enrofloxacin are:
(1) Cattle. Liver (target tissue): 0.1 ppm desethylene ciprofloxacin (marker residue).
(2) Swine. Liver (target tissue): 0.5 ppm enrofloxacin (marker residue).
(c) Related conditions of use. See §§ 516.812 and 522.812 of this chapter.
Legislative history
This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.